Assay Details
Target Gene Details
Entrez Gene ID: | 7991 |
Gene Name: | tumor suppressor candidate 3 |
Gene Aliases: |
D8S1992, M33, MRT22, MRT7, N33, OST3A |
Location: |
Chr.8:15540087-15766649 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
TUSC3 | NM_006765.3 | NP_006756.2 | ||
NM_178234.2 | NP_839952.1 | |||
BC010370.1 | AAH10370.1 | |||
BT020002.1 | AAV38805.1 | |||
DA796279.1 | ||||
U42349.1 | AAB18374.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1161734 | Chr.8:15533647 - 15548772 on Build GRCh38 | Deletion | TUSC3 |
esv3572557 | Chr.8:15469077 - 15543402 on Build GRCh38 | Loss | TUSC3 |
nsv437055 | Chr.8:15398926 - 15806828 on Build GRCh38 | Loss | TUSC3 |
nsv6089 | Chr.8:15538984 - 15565828 on Build GRCh38 | Deletion | TUSC3 |
esv2759598 | Chr.8:14768691 - 15907197 on Build GRCh38 | Loss | SGCZ TUSC3 MIR383 |
esv3616403 | Chr.8:15528780 - 15600263 on Build GRCh38 | Loss | TUSC3 |
dgv248e55 | Chr.8:14773418 - 15806518 on Build GRCh38 | Loss | SGCZ TUSC3 MIR383 |
nsv517314 | Chr.8:15531057 - 15554099 on Build GRCh38 | Loss | TUSC3 |
nsv610466 | Chr.8:14469128 - 15809390 on Build GRCh38 | Loss | SGCZ TUSC3 MIR383 |
nsv818605 | Chr.8:14773392 - 15802730 on Build GRCh38 | Loss | SGCZ TUSC3 MIR383 |
nsv610524 | Chr.8:15419198 - 15568674 on Build GRCh38 | Loss | TUSC3 |
nsv1029399 | Chr.8:14978756 - 16296799 on Build GRCh38 | Gain | MSR1 SGCZ TUSC3 |
nsv8298 | Chr.8:14772387 - 15806223 on Build GRCh38 | Gain+Loss | SGCZ TUSC3 MIR383 |
nsv1020054 | Chr.8:15444894 - 15812092 on Build GRCh38 | Gain | TUSC3 |
nsv465554 | Chr.8:15537635 - 15554099 on Build GRCh38 | Loss | TUSC3 |
More Information
Additional Information:
For this assay, SNP(s) [rs112256089] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |